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Interneuron migration defects during corticogenesis contr... | ResearchHub
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Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis via actomyosin dynamics deregulations
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Authors
Maria HINCKELMANN
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Maria HINCKELMANN
•
María-Victoria Hinckelmann
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•
Yann Hérault
Published
November 10, 2023
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Topics
Biology
Neuroscience
Developmental Biology
Genetics
Gene
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DOI
10.1101/2023.11.09.566424
License
CC-BY-NC
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Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Neuroscience
Developmental Biology
Genetics
Gene
Show all topics
DOI
10.1101/2023.11.09.566424
License
CC-BY-NC
Other Formats
PDF